Events

Retiro De Equipo (Recall) de Device Recall Signature

Según U.S. Food and Drug Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en United States que fue producido por Materialise USA LLC.

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
    Recall
  • ID del evento
    67039
  • Clase de Riesgo del Evento
    Class 2
  • Número del evento
    Z-0628-2014
  • Fecha de inicio del evento
    2013-11-26
  • Fecha de publicación del evento
    2014-01-03
  • Estado del evento
    Terminated
  • País del evento
    United States
  • Fecha de finalización del evento
    2014-01-14
  • Fuente del evento
    USFDA
  • URL de la fuente del evento
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=124626
  • Notas / Alertas
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Notas adicionales en la data
    Prosthesis, knee, femorotibial, semi-constrained, cemented, metal/polymer - Product Code HRY
  • Causa
    Shipped femur guide contained a non-conformance which could possibly impact fit of the drill insert.
  • Acción
    Materialise USA LLC notified the Field Representative on November 26, 2013 of the recall by phone followed by E-mail notification. The notification identified the device and reason for the recall. Notification directions included instructions to find and quarantine the device and return it Materialise. A replacement device was shipped November 27, 2013 receiving the defective device was called, followed by E-mail notification the Recall, which identified the device, problem, and instructed the distributor to find and quarantine product. For questions regarding this recall call 734-662-5057.

Device

Device Recall Signature
  • Modelo / Serial
    Lot 094929
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    US Distribution: MO only.
  • Descripción del producto
    REF 42-411571 QTY 1 CATALOG CAUTION. SEE INSTRUCTIONS FOR USE || SIGNATURE || M PKA GDE/MDL SET SML-MP || DD.....R-FEB55RKA-T JA-A01 05551 || PKA POST CUT SML-PKA MICROPLASTY || CUSTOM-MADE DEVICE || non-sterile || The Signature Personalized Patient Care System includes the patient-specific Signature Guides which are patient specific instruments (guides are considered custom-made per EU definition) intended for use during the surgical procedure for total and partial knee arthroplasty.
  • Manufacturer
    Materialise USA LLC

Manufacturer

Materialise USA LLC
  • Dirección del fabricante
    Materialise USA LLC, 44650 Helm Ct, Plymouth MI 48170-6061
  • Empresa matriz del fabricante (2017)
    Materialise Nv
  • Source
    USFDA